X-ray structure and temperature dependent luminescent properties of two bimetallic europium complexes

Polyhedron ◽  
2008 ◽  
Vol 27 (3) ◽  
pp. 1061-1069 ◽  
Author(s):  
Shawn Swavey ◽  
Jeanette A. Krause ◽  
Daniel Collins ◽  
Deepika D’Cunha ◽  
Albert Fratini
2003 ◽  
Vol 796 ◽  
Author(s):  
Vladimir Vasilyev ◽  
Alvin Drehman ◽  
Lionel Bouthillette

ABSTRACTCorrelations between synthesis conditions, phase composition, and spectral properties of the sintered ceramic, thin films and single crystals of EuTa7O19 phosphors have been studied using x-ray diffractometry and temperature dependent photoluminescence (PL) spectroscopy at temperatures between 18 K and 650 K. From the PL spectra of Eu3+, one can obtain information about the area of homogeneity of phases, their temperature transformations, and changes in the bonding character in the neighborhood of the luminescent ion. As a result, this information helps to optimize the synthesis parameters for luminescent materials.


Coatings ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 403
Author(s):  
Zijun Chen ◽  
Huiyi Xu ◽  
Chunyan Cao ◽  
Xiaoting Chen ◽  
Min Zhang ◽  
...  

In this paper, Sm3+ doped Lu2W0.5Mo0.5O6, Lu2WMoO9, and Lu2(W0.5Mo0.5O4)3 materials were synthesized by using a two-step solid-state reaction method. The synthesized materials were characterized by X-ray diffraction (XRD) patterns, field emission scanning electronic micrograph (FE-SEM) pictures, photoluminescence (PL) excitation and emission spectra, and temperature-dependent emission intensities. Orange-reddish light could be observed from the phosphors under ultraviolet (UV) 365 nm light. The Sm3+ doped Lu2WMoO9 had enhanced PL intensities compared to the other two materials. The excitation, the energy transfer, the nonradiative relaxation, and the emission processes were illustrated by using schematic diagrams of Sm3+ in Lu2MoWO9. The optimal Sm3+ doping concentration was explored in the enhancing luminescence of Lu2WMoO9. By combing the Sm3+ doped Lu2WMoO9 to UV 365 nm chips, near white lighting emitting diode (W-LED) were obtained. The phosphor can be used in single phosphor-based UV W-LEDs.


2008 ◽  
Vol 8 (8) ◽  
pp. 3959-3966 ◽  
Author(s):  
Huihui Liu ◽  
Hongwei Song ◽  
Suwen Li ◽  
Xinguang Ren ◽  
Shaozhe Lu ◽  
...  

To modify the photoluminescence properties the Eu(DBM)3 bath complexes were encapsulated into the sub-nanometer pores of aluminosilicates zeolites L and Yand characterized by X-ray diffraction (XRD), transmission electron micrographs (TEM), Fourier transform infrared spectroscopy (FTIR) and ultraviolet-visible (UV-vis) absorption spectra. The luminescent properties of the encapsulated composites (Eu-L and Eu-Y) were systematically studied. The results indicate that in both the two composites the crystal-field symmetry becomes lower, as a consequence, the 5D0-7F2 electronicdipole transition relative to the 5D0-7F1 magnetic-dipole transition of Eu3+ increases in contrast to the pure complexes. The outer quantum efficiency of the Eu3+ emission and the photostability of Eu3+ are both improved considerably. The adsorption of water in the composites has influence on the thermostability and decay dynamics of the Eu3+ emission. In the composite Eu-L, which contains less water the thermostability of luminescence is improved considerably and the lifetime becomes longer in comparison to the pure complexes. Overall, zeolite L is a more ideal host material for modification of lanthanide complexes.


2021 ◽  
Author(s):  
Yan Chen ◽  
Yuemei Lan ◽  
Dong Wang ◽  
Guoxing Zhang ◽  
Wenlong Peng ◽  
...  

A series of Gd2-xMoO6:xEu3+(x=0.18-0.38) nanophosphors were synthesized by the solvothermal method. The properties of this nanophosphor were characterized by x-ray diffraction (XRD), transmission electron microscope (TEM), fluorescence spectra and diffuse...


Author(s):  
Simon Engelbert ◽  
Rolf-Dieter Hoffmann ◽  
Jutta Kösters ◽  
Steffen Klenner ◽  
Rainer Pöttgen

Abstract The structures of the equiatomic stannides RERhSn with the smaller rare earth elements Y, Gd-Tm and Lu were reinvestigated on the basis of temperature-dependent single crystal X-ray diffraction data. GdRhSn crystallizes with the aristotype ZrNiAl at 293 and 90 K. For RE = Y, Tb, Ho and Er the HP-CeRuSn type (approximant with space group R3m) is already formed at room temperature, while DyRhSn adopts the HP-CeRuSn type below 280 K. TmRhSn and LuRhSn show incommensurate modulated variants with superspace groups P31m(1/3; 1/3; γ) 000 (No. 157.1.23.1) (γ = 3/8 for TmRhSn and γ = 2/5 for LuRhSn). The driving force for superstructure formation (modulation) is a strengthening of Rh–Sn bonding. The modulation is expressed in a 119Sn Mössbauer spectrum of DyRhSn at 78 K through line broadening.


2021 ◽  
Vol 234 ◽  
pp. 117957
Author(s):  
D.S. Arteev ◽  
A.V. Sakharov ◽  
A.E. Nikolaev ◽  
W.V. Lundin ◽  
A.F. Tsatsulnikov

2012 ◽  
Vol 217-219 ◽  
pp. 733-736
Author(s):  
Xiu Mei Han ◽  
Shu Ai Hao ◽  
Ying Ling Wang ◽  
Gui Fang Sun ◽  
Xi Wei Qi

Zn2SiO4:Eu3+, Dy3+ phosphors have been prepared through the sol-gel process. X-ray diffraction (XRD), thermogravimetric and ddifferential thermal analysis (TG-DTA), FT-IR spectra and photoluminescence spectra were used to characterize the resulting phosphors. The results of XRD indicated that the phosphors crystallized completely at 1000oC. In Zn2SiO4:Eu3+,Dy3+ phosphors, the Eu3+ and Dy3+ show their characteristic red(613nm, 5D0-7F2), blue (481nm, 4F9/2–6H15/2) and yellow (577nm, 4F9/2–6H13/2) emissions.


2013 ◽  
Vol 68 (9) ◽  
pp. 971-978 ◽  
Author(s):  
Inga Schellenberg ◽  
Ute Ch. Rodewald ◽  
Christian Schwickert ◽  
Matthias Eul ◽  
Rainer Pöttgen

The ternary antimonides RE4T7Sb6 (RE=Gd-Lu; T =Ru, Rh) have been synthesized from the elements by arc-melting and subsequent annealing in an induction furnace. The samples have been characterized by powder X-ray diffraction. Four structures were refined on the basis of single-crystal X-ray diffractometer data: U4Re7Si6 type, space group Im3m with a=862.9(2) pm, wR2=0.0296, 163 F2 values for Er4Ru7Sb6; a=864.1(1) pm, wR2=0.1423, 153 F2 values for Yb4Ru7Sb6; a=872.0(2) pm, wR2=0.0427, 172 F2 values for Tb4Rh7Sb6; and a=868.0(2) pm, wR2=0.0529, 154 F2 values for Er4Rh7Sb6, with 10 variables per refinement. The structures have T1@Sb6 octahedra and slightly distorted RE@T26Sb6 cuboctahedra as building units. The distorted cuboctahedra are condensed via all trapezoidal faces, and this network leaves octahedral voids for the T1 atoms. The ruthenium-based series of compounds was studied by temperature-dependent magnetic susceptibility measurements. Lu4Ru7Sb6 is Pauli-paramagnetic. The antimonides RE4Ru7Sb6 with RE=Dy, Ho, Er, and Tm show Curie-Weiss paramagnetism. Antiferromagnetic ordering occurs at 10.0(5), 5.1(5) and 4.0(5) K for Dy4Ru7Sb6, Ho4Ru7Sb6 and Er4Ru7Sb6, respectively, while Tm4Ru7Sb6 remains paramagnetic. Yb4Ru7Sb6 is an intermediate-valent compound with a reduced magnetic moment of 3.71(1) μB per Yb as compared to 4.54 μB for a free Yb3+ ion


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